New monoclonal antibodies against the receptor dec-205 of chicken dentritic cells

ABSTRACT

The invention relates to the production and the characterisation of new murine monoclonal antibodies that recognize the domain CTD-2 (SEQ ID NO: 1) of the cell receptor DEC-205 of dendritic cells in chickens ( Gallus gallus ), pigs, ( Sus scrofa ) and humans ( Homo sapiens ). The invention also relates to the capacity of the new antibodies to direct and modulate the immune response at different levels in chickens ( Gallus gallus ) and pigs ( Sus scrofa ), as well as recognising the receptor DEC-205 in dentritic cells and cell lines in humans, In addition, the invention is used to quickly produce a specific humoral immune response against Hemaglutinina H5 of the H5N2-type avian flu virus.

TECHNICAL SCOPE

This invention pertains to the production and characterization of new murine monoclonal antibodies that recognize the CTLD-2 domain (SEQ ID NO: 1) of the DEC-205 cellular receptor of dendritic cells in chickens (Gallus gallus), pigs (Sus scrofa), and humans (Homo sapiens). This invention pertains to producing new monoclonal antibodies from hybridomas that are created by fusing SP2 myeloma cells with spleen cells of BALB/c rats that have been immunized with the CTLD-2 (SEQ ID NO: 1) fragment of avian origin of this receptor. The invention also pertains to the capability of the new antibodies to direct and significantly modulate the immune response at different levels in chickens (Gallus gallus) and pigs (Sus scrofa), as well as to recognize the DEC-205 receptor in dendritic cells and cell lines of human origin. In addition, there is a brief description of the application of this invention in obtaining a specific humoral immune response over the short term against hemagglutinin H5 (SEQ ID NO: 8) of the H5N2 avian flu virus.

BACKGROUND TO THE INVENTION

The immune system has highly specialized cells for carrying out various processes; among them dendritic cells (DCs) have the ability to stimulate the primary and secondary responses of the B and T lymphocytes, as well as the response of T cytotoxic lymphocytes in rats and human lymphocytes (Carter et al., 2006). This capability is due to the fact that DCs are the cells that are most highly specialized in the presentation of antigens, internalizing, processing, and presenting them in the form of peptides combined with the molecules of the major histocompatibility complex class II (MHC-II). They originate from the myeloid progenitor cells, which are capable of differentiating themselves into immature dendritic cells and ultimately into mature dendritic cells by expressing various surface markers. The function as an antigen present or of dendritic cells has been connected to high levels in the expression of the DEC-205 receptor, also called CD205 or lymphocytic antigen 75, especially in dendritic cells located in areas of T cells of peripheral or secondary lymph organs (Jiang et al., 1995; Kraal et al., 1986; Winter-Pack et al., 1995). This was substantiated by the internalization of human anti-DEC-205 receptor dendritic cells (Bonifaz et al., 2002; Steinman and Banchereau, 2007; Steinman, 2008; Ueno et al., 2010). The DEC-205 receptor is an endocytic receptor with a broad extracellular domain that contains various subdomains: a cysteine-rich (CR) domain, a fibronectin type II (FN) domain and 10 contiguous carbohydrate recognition domains (CRDs), also known as C-type lectin domains (or CTLDs in the English acronym) (Mahnke et al., 2000). These multi-lectin domains affect the efficiency of the processing and presentation of antigens in vivo (Hawiger et al., 2001). Other examples of C-type lectin receptors include Langerina, DC-SIGN, mannose receptor and A₂ phospholipase receptor, which have also been implicated in antigen processing and presentation (Figdor et al., 2002; Idoyaga et al., 2008).

It should be noted that the pioneering experiments that described the cellular processes of directing an antigen were carried out using the DEC-205 human receptor, where the T-cell-mediated response changes dramatically when the maturation stimulus of the dendritic cells is added at the same time as the directing of the antigen using an antibody directed against the DEC-205 receptor (Bonifaz et al., 2002; Hawiger et al., 2001). The proliferation of T cells increases by various orders of magnitude when compared to a classic immunization protocol. It has also been observed that, when the antigens are directed at the dendritic cells via DEC-205, there is an increase in the stimulation of the cooperating T cells (Th); this makes it possible or promotes the humoral immune response or antibody production (Bonifaz et al., 2004; Boscardin et al., 2006). In point of fact, the directing of antigens using this marker and CD11c has increased the kinetics of the production of high-titer antibodies during the first seven days after immunization (Wang et al., 2000; Cheong et al., 2010). Moreover, the presence of the DEC-205 receptor has been described in lines other than human dendritic cells, such as in B cells, T cells, NK cells, and monocytes (Kato et al., 2006); cerebral capillaries, stroma of the medulla ossea, and cortical epithelium of the thymus; they are also found in other species of mammals such as chimpanzees and rats and in other non-mammalian species (Kraal et al., 1986; Witmer-Pack et al., 1995), including chickens (Gallus gallus).

DEC-205 Receptor of Gallus gallus

The genome and protein sequences for the DEC-205 receptor of Gallus gallus has been reported in the European Nucleotide Archive (http://www.ebi.ac.uk/ena/, access number AJ574899; in the ENSEMBL database (http://www.ensembl.org/), in the GenBank (http://www.ncbi.nlm.nih.gov), access number NP_001032925.1), and in the UniProtKB/TrEMBL, where it has access number Q4LDF5. These databases report the presence of 35 exons that have codifying sequences; these make up the domains of the DEC-205 receptor of chickens, represented as N-CRD-FNII-CTLD1-CTLD2-CTLD3-CTLD4-CTLD5-CTLD6-CTLD7-CTLD8-CTLD9-CTLD10-TMC, where N is the N-terminal region, CRD represents the cysteine-rich domain, FNII represents the type II fibronectin domain, CTLD1 to CTLD10 represent the 10 “type-C lectin domains”, and TMC represents the transmembrane and cytoplasmic domains (FIG. 1).

In recent years investigation into dendritic cells has been focused mainly on the application of new clinical procedures, in particular the implementation of new tools that enhance the immune response within short periods of time.

Antibodies

The use of antibodies or immunoglobulins that recognize the surface receptors of dendritic cells is based on the ability of these molecules to interact in a specific manner and with high affinity for the immunogens against which they are produced. The antigens are glycoproteins that comprise two heavy chains and two light chains that are interconnected by disulfide bridges to an antigen union region. The heavy chains have a variable region (V_(H)) and a constant region (C_(H)), with the latter being able to present 3-4 domains, which intervene directly in the union with cells of the immune system or with the complement system (Padlan, 1994). However, the light chains comprise a variable region (V_(L)) and a constant region which has a single domain C_(L). The variable regions (V_(H) and V_(L)) contain the antigen union site, referred to as hypervariability regions or complementarity-determining regions (CDR). These regions are interspersed with more conservative regions that are called marker or “framework” regions (FR).

The antibodies that exhibit a high degree of union specificity and affinity for an epitope are the monoclonal antibodies, which are produced by a hybridoma that is generated by the fusion of immortalized cells (myeloma), which do not secrete immunoglobulins, and B cells obtained from the spleens of rats immunized against an antigen that contains the information of the heavy and light chains.

Combined with monoclonal interbody technology, in the state of the art, it is possible to obtain the genes that codify the variable domains of all possible immunoglobulins by rearranging the nucleotide sequences. This can be obtained from the lymphocytes of any vertebrate, including human beings. In reality, right now it is possible to select only the variable elements of the heavy and light chains of the antibodies, which can be united by a connector peptide in such a way as to produce a fragment of a single chain of the antibodies, which are able to recognize the antigens. Our group was able to prepare a bank of genes that express the single-chain fragments and, by means of the filamentous-phage deployment technique, it was possible to obtain antibodies that protect against toxins of scorpion venom (Riaño-Umbarilla et al., 2005, see also U.S. Pat. No. 7,381,802 B2, Jun. 3, 2008). An idea that underlies these advances in the technique and is complementary to this invention is to obtain single-chain fragments of human antibodies for the purpose of applying the same principle as described here, against possible antigens that cause health problems in humans (Rodriguez-Rodriguez et al., 2012). In other words, the idea is to obtain by genetic engineering the variability in single chains of human antibodies for possible application in the development of vaccines.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 depicts in schematic form the different domains of the DEC-205 receptor; the latter belongs to the type C family of lectins. In the amino-terminal region (N) is the cysteine-rich domain (CRD), followed by a fibronectin domain type II (FNII) and 10 “type C lectin domains” (CTLD-1 to CTLD-10). In the carboxyl-terminal region the transmembrane and cytoplasmic (TMC) domains are represented.

FIG. 2 shows the expression vector (pET22b) indicating various loci that are present, as well as the location of the CTLD-2 gene. A: His-Tag; B: stop codon; and C: origin of F1.

FIG. 3 shows some of the steps in the process of purification of the CTLD-2 domain in 12% SDS gel electrophoresis.

FIG. 4 A) shows the titer of the polyclonal serum of two rats that were immunized with the CTLD-2 recombinant immunogen, compared to pre-immune polyclonal serum. The logarithm of the dilution is plotted on the abscissa, and absorbency at 405 nm is plotted on the ordinate; (a): pre-immune serum; (b): serum from rat 1 and (c) serum from rat 2. B) shows a graphic of the union of the two anti-CTLD-2 murine antibodies using supernatant from the hybridomas obtained by the indirect ELISA technique. On the abscissa are the different hybridomas obtained, and absorbency at 405 nm is plotted on the ordinate. C): shows the recognition of the monoclonal antibodies 2F2E8E3B4, 2F2E8E3B6, 4D12R, and 4D12F4 toward the CTLD-2 domain by indirect ELISA. On the abscissa are the various monoclones obtained, and on the ordinate absorbency at 405 nm is plotted.

FIG. 5 shows the titer of the monoclonal antibody 2F2E8E3B6 compared to the supernatant of the SP2 cells. The dilution logarithm is plotted on the abscissa, and absorbency at 405 nm is plotted on the ordinate; (a): AbM 2F2E8E3B6, and (b): supernatant of the SP2 cells.

FIG. 6 shows the immunoprecipitation of lysed cells of chicken (Gallus gallus) spleen using the anti-CTLD-2 murine monoclonal antibodies. The specific immune-isolation of the DEC-205 receptor (205 kDa) present in white chicken spleen cells in a gel SDS-PAGE at 10% under reduction conditions compared to a negative control (left-hand track) is observed. The electrophoretic run of the heavy chain (50 kDa) and light chain (25 kDa) of the 2F2E8E3B6 antibody is also observed. Con: Control.

FIG. 7 shows the internalization of the chicken DEC-205 receptor using the anti-CTLD-2 antibodies in the cell line of T lymphocytes (Jurkat) using intracellular staining analyzed by flow cytometry. 7A shows the control, and 7B shows the cells after 30 minutes of incubation with the anti-CTLD-2 antibody; on average a percentage of 13.91% of the cells that internalize the white of the antibody is observed. Co: count, and (a): PE cells.

FIG. 8 shows the titers of IgY with respect to avian hemagglutinin H5, monitored by Western Blot.

FIG. 9 shows the titers of IgY with respect to avian hemagglutinin H5 after intradermal immunization of two hens. The IgYs obtained from the yolks of the eggs 15, 18, and 21 days after immunization are compared to the IgYs of control hens. The dilution logarithm is plotted on the abscissa, and absorbency at 405 nm is plotted on the ordinate. G1: hen 1; G2: hen 2; (a): preimmune serum; (b): 15 days; (c): 18 days; and (d): 21 days.

FIG. 10 A) shows the recognition of the lymphocytic receptor 75 (DEC-205) in species other than Gallus gallus, such as Homo sapiens (human) and Sus scrofa (pig) by means of immunoprecipitation using the anti-CTLD-2 antibody 2F2E8E3B6. B) shows the alignment of sequences of the CTLD-2 segment 2F2E8E3B6 of the lymphocytic antigen 75 of Gallus gallus (NP_001032925.1) compared to the sequences of Homo sapiens (NP_002340.2) and the pig (Sus scrofa) (NP_001171875.1), as well as their percentage of identity.

DETAILED DESCRIPTION OF THE INVENTION

This invention provides new monoclonal antibodies of murine origin that are capable of recognizing the DEC-205 receptor of Gallus gallus, which has properties that are particular and specific to the immunological level in dendritic cells. Thus, the antibodies that are produced have the potential to be used in a variety of directed immunologic processes, such as affecting the ability to present different antigens, inducing the response of T cells, or increasing the proportion of antibodies produced against a variety of specific avian pathogens. Various aspects of the invention are described in detail in the following sections.

DEFINITIONS

The expressions “cell” and “cell culture” as used here are employed as synonyms, and all of these designations include offspring. Thus, the words “transformants” and “transformed cells” include the primary subject cell and cultures derived therefrom without considering the number of transfers. It is also understood that not all offspring have to be exactly identical with regard to their DNA content due to deliberate or accidental mutations. This includes mutant offspring that have the same function or biological activity as that detected in the originally transformed cell. When different designations are intended, these should be clear from the context.

The term “effective quantity” or “pharmacologically effective quantity” of a compound in a single dose of the mixture depends on various factors. These factors include the amounts of other ingredients in the case where they are used and tolerance to the active ingredient of the compound.

“Pharmaceutically acceptable vehicle” refers to the filler or diluent solids or liquids or substances that can be safely used when administered systemically or topically. Depending on the particular pathway of administration, various vehicles that are well known in the industry and that include filler or diluent solids or liquids, hydrotropes, surfactants, and encapsulating substances are pharmaceutically acceptable. The amount of vehicle used along with the monoclonal antibodies provides a manageable dose of material per single dose of the compound.

Pharmaceutically acceptable vehicles for systemic administration that can be incorporated into the compound of the invention include sugar, starches, cellulose, vegetable oils, buffers, polyols, and alginic acid. Specific pharmaceutically acceptable vehicles are described in the following documents, all of which are mentioned here as references: U.S. Pat. No. 4,401,663, Buckwalter et al., granted on Aug. 30, 1983; European Patent Application number 089710, LaHann et al., published on Sep. 28, 1983, and European Patent Application number 0068592, Buckwalter et al., published on Jan. 5, 1983. The vehicles that are preferred for parenteral administration are polypropylene glycol, pyrrolidine, ethyl oleate, aqueous ethanol, and combinations thereof.

Representative vehicles include gum arabic, agar, alginates, hydroxyalkyl cellulose, hydroxypropyl methyl cellulose, carboxymethyl cellulose, sodium carboxymethyl cellulose, carrageenan, powdered cellulose, guar gum, cholesterol, gelatin, gum agar, gum arabic, karaya gum, gum ghatti, locust bean gum, octoxynol-9, oleyl alcohol, pectin, polyacrylic acid and its homologues, polyethylene glycol, polyvinyl alcohol, polyacrylamide, sodium lauryl sulfate, polyethylene oxide, polyvinylpyrrolidine, glycol monostearate, propylene glycol monostearate, gum xanthan, tragacanth, sorbitan esters, stearic alcohol, and starch and modifications thereof. The adequate ranges vary from 0.5% to 1%.

1. Immunogens of DEC-205

-   -   Using homology modeling (with the EsyPred3D and SWISS-MODEL         Repository programs) of all of the domains of DEC-205 and taking         as molds structures of the homolog domains previously reported         (www.pdb.org), the domains that had greater exposure to the         solvent, as well as the sites that were involved in the union to         ligands in the structure of chicken DEC-205 (Jiang et al. 1995),         were located. The domains that were selected to be cloned and         expressed in a heterologous system were the following:     -   1. Cysteine-rich domain (CRD, cysteine rich domain), located in         the amino-terminal region of the extracellular side of the         DEC-205 receptor (see FIG. 1).     -   2. Fibronectin (FN) type II domain, located in the         amino-terminal region of the extracellular side of the DEC-205         receptor (see FIG. 1).     -   3. Type C lectin-like domain 2 (CTLD-2, C-Type Lectin-Like         Domain-2), located on the extracellular side of the DEC-205         receptor and involved in the union with carbohydrates (Jiang et         al. 1995) (see FIG. 1).     -   To carry out the cloning of these fragments, the introns and         exons of the genes of each of the domains selected were analyzed         using the Wise2 program         (http://www.ebi.ac.uk/Tools/Wise2/index.html) and the Artemis         program (http://www.sanger.ac.uk/resources/software/artemis/).         Of the three domains selected, only the CTLD-2 domain was cloned         and expressed satisfactorily in large quantities.

2. Cloning and Expression of the CTLD-2 Domain

This invention undertakes the recombinant production of the CTLD-2 domain of the DEC-205 receptor of Gallus gallus, the domain selected as an immunogen for generating monoclonal antibodies because it provided easier access for foreign molecules since it is located on the extracellular surface of the DEC-205 receptor and cloning and recombinant expression thereof proved to be satisfactory. For this purpose, using genomic DNA obtained from the peripheral blood of a healthy chicken, the exons of this domain were isolated with the specific oligos CTLD-E1FNco, CTLD-E1R, CTLD-E2F, CTLD-E2R, CTLD-E3F, CTLD-E3RHin (SEQ ID NO: 2, 3, 4, 5, 6, and 7, respectively), and they were then assembled, cloned in the pET-22b(+) vector (FIG. 2), and transformed for recombinant expression thereof in the Rosetta II strain of E. coli. After they were expressed, they were purified (FIG. 3) and characterized in order to be used as an immunogen, as detailed in Example 1.

3. Immunization of BALB/c Rats with the Recombinant CTLD-2 Domain

The immunization with the CTLD-2 recombinant domain was done intraperitoneally (IP) by administering to five rats increasing concentrations of antigen (25, 50, 100, 150, and 200 μg) with a complete Freund adjuvant at a ratio of 1:1 (100 μL total volume), followed every 10 days by IP administration of the antigen alternatingly mixed with incomplete adjuvant or alumina (at a ratio of 1:1) (up to a total of five immunizations). The immune response was monitored during the immunization protocol by taking samples of murine serum obtained from the retro-orbital complex during the fourth immunization. These samples were analyzed by the indirect ELISA method (FIG. 4A), where the rats with high titers of anti-DEC-205 chicken antibodies were used to fuse with the immortalized spleen cells. The rats were reinforced by IP with antigen one or two days before they were sacrificed and their spleens were removed.

4. Generation and Production of the Antibodies that Recognize DEC-205

This invention undertakes to generate murine monoclonal antibodies that are capable of recognizing the DEC-205 receptor of Gallus gallus via the CTLD-2 domain (SEQ ID NO. 1). The monoclonal antibodies that were united with DEC-205 with high recognition included those produced by a hybridomas of the 4D12 and 2F2 families (FIG. 4B), which were produced as shown in detail in Example 2, in accordance with well-standardized protocols (Koehler and Milstein, 1975; Goding, 1986).

After the hybridomas were identified as producers of the antibodies with the desired specificity, sub-cloning was done by limiting dilution and growth in the D-MEM medium under standard conditions (Goding, 1986). In cases where four monoclones, 2F2E8E3B4, 2F2E8D3B6, 4D12R, and 4D12F4 presented high recognition for the CTLD-2 domain, which was identified by the indirect ELISA method (FIG. 4C) [translator's note: incomplete sentence]. The isotypes of the monoclonal antibodies obtained were determined by sandwich ELISA using the culture supernatants of the hybridomas and the commercial Mouse Typer Sub-Isotyping kit (Bio Rad). In addition, the hybridomas were grown in vivo inducing liquid tumors (ascites) in various rats of the BALB/c strain in order to produce sufficient quantities of antibodies.

The monoclonal antibodies secreted by the hybridomas were separated from the ascitic fluid and from the growth medium by conventional procedures for purification of immunoglobulins such as affinity chromatography using Protein A-Sepharose, as illustrated in Example 3. The ones in which greater yields were obtained during the purification process were selected for the purpose of determining their EC₅₀ (FIG. 5), and the sequencing of the variable light and heavy chains of these antibodies was then done (Example 12).

5. Functional Characterization of the Anti-DEC-205 Monoclonal Antibodies

In order to determine whether the anti-CTLD-2 monoclonal antibodies unite with the DEC-205 receptor as expressed in live cells of Gallus gallus and other species and whether these antibodies make it possible for the receptor to operate in the internalization and processing of antigens the techniques of flow cytometry and immunoprecipitation were used, as illustrated in Examples 5, 6, and 10. For instance, use was made of the clear lysates of white cells that had been previously purified from various organs and various cell lines in which the presence of the DEC-205 receptor was determined by the immunoprecipitation technique, using the monoclonal antibody with greater recognition as determined by this invention, 2F2E8E3B6, at saturating concentrations. After incubation was done with the primary antibody, a second phase was carried out in which the Sepharose-Protein A resin (Pierce, Rockford, Ill., USA) was added; this complex made the antibody insoluble once united with the protein A, making it possible to separate the antibody with its specific target by centrifuging and to analyze this interaction by SDS-PAGE. As an example of this, FIGS. 6 and 10A are presented in which the presence of a band at 205 kDa is observed that is approximately recognized by the monoclonal antibodies produced in this work, indicating the presence of the DEC-205 receptor in the spleen cells of Gallus gallus and Sus scrofa and in cell lines of Homo sapiens. On the other hand, using cellular preparations in which the presence of the DEC-205 receptor and monoclonal antibodies of the 2F2 anti-CTLD-2 monoclonal antibodies was identified, an analysis was made of the internalization of these antibodies via their target by determining the presence of these antibodies, located intracellularly, using flow cytometry (Example 6, FIG. 7). In the case of the antibodies that were used, their presence was observed inside the cells that were used, confirming the process of internalization.

6. Obtaining Hemagglutinin 5 from the H5N2 Avian Flu Virus

This invention used the RNA of the type H5N2 avian flu virus obtained from a collection of RNAs donated by Dr. R. Webster (St. Jude Hospital, Tennessee, USA) in order to isolate the gene that contains the hemagglutinin H5 (SEQ ID. NO: 8), the antigenic determining principal for developing the pathogenesis of the flu virus, as well as cloning and expressing it heterologically using the baculovirus system, which is described in Example 7.

7. Molecular Conjugates with the Monoclonal Antibodies

The possibility of obtaining a very wide variety of molecular conjugates that are generally based on an antigen united with the monoclonal antibodies of the present invention that are capable of recognizing the DEC-205 receptor that is present in chicken antigen presenting cells (CPA) [translator's note: incomplete sentence]. This makes it possible to direct the antigen to the CPAs to step up the processing, presentation, and immune response against the antigen, for example, the release of immuno-stimulating cytokines or an increase in the humoral response. These anti-CTLD-2 antibodies can be united with cells or pathogens by means of chemical “linkers” or by any other related method such as those described by Kruif et al., 2000, and Nizard et al., 1998. In Example 8 a description is given of the conjugation or coupling procedure used. Briefly, the monoclonal antibodies were activated with succinimidyl-4-(N-maleimidomethyl) cyclohexane-1-carboxylate (SMCC; Pierce, Rockford, Ill., USA), which adds maleimide and ester groups to the proteins that make covalent conjugation possible with molecules that contain sulfhydryl or amino groups, while the antigen used, the recombinant protein of hemagglutinin H5 (SEQ. ID NO:8) of the avian flu virus was modified with 2-iminothiolane (Traut, Pierce, Rockford, Ill., USA), which is reactive and which reacts with primary amines to introduce sulfhydryl groups at these sites, generating target sites for the modified antibodies and carrying out covalent conjugation, as detailed in Example 8.

8. Effect Analysis in the Immune Response in Birds from the Immunization of the Molecular Conjugate Anti-DEC-205 Antibodies-H5 Hemagglutinin

To carry out this analysis, two egg-laying hens of the Rhode Island Red type, 25 weeks old, were immunized with the Ab 2F2E8D3B6-Hemagglutinin H5 conjugate mixture. Then IgYs were purified from the egg yolks in order to determine the titers of the Hemagglutinin H5 (SEQ. ID NO:8) chicken antibodies (IgYs) by means of indirect ELISA (see Example 9). The hens successfully generated antibodies that were capable of recognizing the viral protein with larger titers compared to the control starting at day 15 (FIG. 9), confirming that the anti-CTLD-2-Hemagglutinin H5 conjugates of this invention have the potential to be used to generate an effectively rapid immune response with the generation of antibodies that protect against possible viral infections.

9. Uses of the Invention

The proposal of this invention extends to veterinary uses, especially for fattening chickens and egg-laying hens using the species Gallus gallus as a model, due to the fact that the movement of these specimens from production areas to consumption areas can form foci for the spread of contagious diseases. This proposal uses the DEC-205 receptor of Gallus gallus as a modulator of the immune response since the molecules that specifically recognize dendritic cells by means of this receptor, as specific antibodies directed against the complete protein or one of its domains, have the potential to direct the immune response at different levels and to produce a potent immune response against the antigens that are united with these antibodies, by means of chemical conjugation or genetic engineering. It is thus possible to speed up the immune response against innumerable specific infections among these birds.

The molecular conjugates of this invention have the ability to be used to treat or prevent a variety of diseases and/or specific conditions in the species Gallus gallus and in animals in which there exists cross-reactivity in recognition by means of this receptor. The viral antigen-antibody conjugates can be used to prevent viral illnesses such as avian smallpox, Newcastle disease, coronavirus, enterovirus, etc. Likewise, bacterial antigen-antibody conjugates can be used to prevent bacterial illnesses such as avian cholera or infectious coryza. For example, using the Cp39 protein of Pasteurella multocida for the case of avian cholera (Sthitmatee et al., 2008) or the protein of the HMTp210 external membrane (210 kDa) of Avibacterium paragallinarum, which produces infectious coryza (Sakamoto et al., 2012) [translator's note: incomplete sentence]. Likewise, some viral agents that cause cancer in this species of animal can be used as antigens to make the conjugates, for example, the gp85 protein of the subgroup J avian leukosis virus (Sun et al., 2012).

Among these diseases, the highly pathogenic avian flu seriously affects poultry farmers wherever it presents, with the always-present possibility of a pandemic, which would be devastating both to the economy and to the populace. As a recent example, in 2012 there was an avian flu outbreak in our country that caused significant economic losses to Mexican aviculture. This invention used Hemagglutinin H5, the principal antigenic determinant of the H5N2 avian flu, as an antigen that was directed by the new antibodies of this invention produced against domain 2 of type-C lectins of DEC-205 (anti-CTLD-2) upon being conjugated with them.

For use in therapy, the conjugates of this invention may be administered to patients indirectly, for example, by first growing or incubating the conjugates with antigen presenter cells, such as dendritic cells, and then administering them to the patients (ex vivo) (Gunzer and Grabbe, 2001; Steinman, 1996; Tacken et al., 2006; Tacken et al., 2007). In all cases the conjugates are administered in quantities that are sufficient to achieve their desired therapeutic effect, for example, to eliminate the bacterial, viral, or fungal infection. The effective quantity for each particular application may vary depending on the illness or condition to be treated. The preferred pathways for administering the conjugates include, for example, subcutaneous or intraperitoneal injection or possibly oral administration if necessary.

EXAMPLES

The following examples are presented by way of illustrating some of the methods for obtaining or utilizing this invention. It is possible to implement many variations on these methods without exceeding the scope of this invention, and therefore they should not be considered limiting in any way.

Example 1 Cloning, Expression, and Purification of the CTLD-2 Domain (SEQ ID NO:1)

The amino-acid sequence of the DEC-205 receptor of Gallus gallus is reported in GenBank (http://www.ncbi.nlm.nih.gov) with access number NP_001032925. 1. In the list of sequences, the CTLD-2 domain that was cloned is presented as SEQ ID NO:1, which was obtained from genomic DNA of the peripheral blood of a healthy chicken using specific oligos CTLD-E1FNco, CTLD-E1R, CTLD-E2F, CTLD-E2R, CTLD-E3F, and CTLD-E3RHin (SEQ ID NO: 2, 3, 4, 5, 6, and 7, respectively) to obtain the three exons that comprise them, which were assembled, cloned, and transformed to provide for their recombinant expression in the Rosetta-II strain of E. coli. FIG. 2 shows in detail the cloning site of CTLD-2 with in the expression vector pET22b(+), which is flanked by the pelB sequence in the amino-terminal region, which directs the recombinant protein toward the bacterial periplasm, in addition to a contiguous sequence of six histidines in the carboxyl-terminal region that are used for its purification, and finally a stop line is attached. This system was optimum for expression in inclusion bodies of recombinant protein CTLD-2 (SEQ ID NO:1) after being induced with IPTG to a final concentration of 0.2 mM once a DO_(600 nm) of 0.7 was reached. After 12 hours of induction, the cellular precipitate was obtained, which was solubilized under denaturing conditions (a buffer of phosphate-TrisHCl, pH 8.0, and 8M of urea), ensonified, and centrifuged. The soluble fraction containing the protein of interest was purified by affinity chromatography using a nickel-NTA-agarose column (Qiagen, USA), with elution being done by changing the pH. FIG. 3 shows some of the steps in the process of the purification of the CTLD-2 domain by affinity chromatography (SEQ ID NO:1) in SDS-PAGE electrophoresis at 12%, stained with colloidal coomassie. Traces: 1) precipitate solubilized in a buffer of phosphate-TrisHCl, pH 8.0, and 8M of urea; 2) first washing with 4M of urea; 3) with 2M of urea; 4) with 0.2M of urea; 5) washing with 25 mM of imidazole; 6) elution 1 with 250 mM of imidazole; 7) elution 2 with 250 mM of imidazole; 8) elution at pH 5.9; 9) elution at pH 4.5; 10) molecular weight markers (Pre-stained Protein Marker Broad Range, New England, Biolabs). Then, the samples that were eluted by changing pH 4.5 were reduced with DTT (Sigma Aldrich, USA), 100 mM for one hour at 52° C., then undergoing a second step of purification by phase-reverse HPLC using a C₁₈ preparation column (Vydac, USA) in a Waters 600E apparatus equipped with an absorbency detector within the ultraviolet (UV) light spectrum, Waters 486 and a Waters 745B graph plotter, with a linear gradient of 20-70% of acetonitrile in the presence of 0.1% trifluoroacetic acid (TFA) at a flow rate of 1.60 mL/minute for a period of 50 minutes, in which the CTLD-2 peak was obtained at a retention time of 33.74. This material, which was subjected to analysis by mass spectrometry, showed that it was homogeneous and had a molecular weight of 21,229 Da, indicating that the domain was united with the signal peptide in accordance with the construct shown in FIG. 2. The concentration of the CTLD-2 protein (SEQ ID NO:1) was determined from the molar extinction coefficient, which was theoretically estimated with the ProtParam server (http://ca.expasy.org/tools/protparam.html). Following this purification protocol, a yield of 1.0 mg of protein of 98% purity was obtained per liter of culture.

Example 2 Generation of Hybridomas that Produce Murine Monoclonal Antibodies Toward DEC-205

In order to generate hybridomas that produce monoclonal antibodies toward DEC-205 of Gallus gallus, five rats were immunized intraperitoneally with the CTLD-2 domain (SEQ ID NO:1) with increasing concentrations of antigen (25, 50, 100, 150, and 200 μg) with a complete Freund adjuvant at a ratio of 1:1, followed every 10 days with IP immunizations of the antigen mixed alternatingly with incomplete adjuvant or alumina (ratio 1:1) (up to a total of five immunizations). After the last immunization, the murine splenocytes were isolated and fused in the presence of 50% PEG (w/v) to an immortal cell line, in this case the SP2 rat myeloma cell line. The fused cells were placed in 96-well plates at 37° C. at 5% CO₂ in 100 μl of a selective HAT medium (Sigma Aldrich, USA); at 48 hours, 100 μL of HT medium was added in order to reduce the concentration of aminopterin with respect to the volume of the culture; after 10 days of growth, the wells were observed where hybridomas had grown and replacement was done with the selective HT medium (Sigma Aldrich, USA). Once extensive growth of the hybridomas had been verified, a sample was taken consisting of 100 μL of the growth medium, and an evaluation was done of the production of murine IgG antibodies that were specific against the CTLD-2 domain by means of the indirect ELISA technique. The results are shown in FIG. 4A, which shows the eight hybridomas with greater recognition by means of ELISA toward the CTLD-2 domain (SEQ ID NO:1); of these, the murine antibodies produced by the 2F2 and 4D12 hybridomas were the ones that exhibited the highest level of recognition by indirect ELISA.

These antibody-secreting hybridomas (2F2 and 4D12) were expanded, reevaluated, and subcloned at least three or four times by limiting dilution. The results are shown in FIG. 4B, which shows that the 2F2E8E3B4, 2F2E8D3B6, 4D12R, and 4D12F4 monoclones had the highest levels of union for the CTLD-2 antigen (SEQ ID NO:1) by indirect ELISA.

Example 3 Production and Purification of Anti-DEC-205 Murine Monoclonal Antibodies

The 2F2E8E3B4, 2F2E8D3B6, 4D12R, and 4D12F4 monoclones were cultivated in vivo in a DMEM medium (Hyclone Laboratories, Thermal Fisher Scientific, USA) with 10% inactivated bovine fetal serum (Byproducts, Mexico), OPI (Sigma Aldrich, USA), and antibiotics (streptomycin/penicillin, Sigma Aldrich, USA) in order to generate antibodies in the supernatant, and they were then characterized and purified. Likewise, in vivo induction of ascitic fluid was done upon inducing liquid tumors by means of intraperitoneal administration of the above-mentioned monoclones in BALB/c rats that were previously stimulated with Pristano (Sigma Aldrich, USA). After a period of 15-20 days, the hybridomas were inoculated, and 8-10 days later the ascitic fluid was milked and kept frozen for subsequent purification and characterization.

The monoclonal antibodies secreted by the hybridomas were separated from the growth medium or ascitic fluid by conventional immunoglobulin purification procedures such as affinity chromatography using Protein A-Sepharose (Pierce, Rockford, Ill., USA). In the case of the clones grown in a growth medium, they were expanded in 75 cm² flat-bottom bottles. The supernatants were filtered, concentrated, and dialyzed against PBS before being purified by affinity chromatography and eluted by pH change using 100 mM of ascitic acid pH 3.0. All of the elution samples were received in Tris 1M pH 8.0 buffer in order to be neutralized. The concentration of protein was determined by DO_(280 nm) using an extinction coefficient of 1.43. The immunoglobulin purification process was verified by SDS-PAGE and ELISA.

Example 4 Characterization of the Monoclonal Antibodies Toward DEC-205 by Indirect ELISA

100 μL/well of the CTLD-2 recombinant antigen (SEQ ID NO:1) was placed in 96-well high-union polystyrene plates, expressed as in Example 1 at a concentration of 3 μg/mL in 50 mM of carbonate buffer and incubated over night at 4° C. The plates were blocked with 5% bovine serum albumin in Tris 50 mM pH 8.0 and with 0.2% Tween 20 for one hour at 37° C. After washing was done three times with a wash solution (Tris 50 mM pH 8, NaCl 150 mM, 0.05% Tween), incubation was done at 37° C. for one hour with serial dilutions of the monoclonal antibodies that were produced and purified as described in Example 3. After the washing operation was repeated, incubation was done for one hour at 37° C. with the secondary anti-rat goat antibody coupled to HRP (1:5000, Zymed Laboratories Incorporated). The ABTS substrate (2.2′-azino-di(3-ethyl-benzothiazoline)sulfonate) (Roche Applied Science, Germany) was used in the revealing process. The reading in units of absorbency was done at 405 nm in the ELISA Tecan Spectra reader. Supernatant from the Sp2 cellular culture was used as a negative control. FIG. 5 shows the titration curve of the 2F2E8E3B6 purified antibody which was done in triplicate, producing an EC₅₀ of 4.4 ng, while the 4D12R had an EC₅₀ of 1.377 μg; therefore the 2F2E8E3B6 antibody turned out to have greater recognition for the CTLD-2 domain.

The isotypes of the monoclonal antibodies that were obtained were determined by sandwich ELISA using the supernatants from the hybridomas and the commercial kit Mouse Typer Sub-Isotyping Kit (BioRad, CA, USA) following the vendor's instructions. The antibodies of the 2F2 family have a heavy chain with the IgG2a isotype and a lambda-type light chain, while the antibodies of the 4D12 family have a heavy chain with the IgG1 isotype and a kappa-type light chain.

Example 5 Immunoprecipitation with Anti-CTLD-2 Antibodies

White cells of the spleens of chickens (Gallus gallus), four weeks old, were stimulated with lipopolysaccharide (LPS, SIGMA Aldrich USA) 200 ng/mL, for 24 hours and were then lysed in an immunoprecipitation buffer (PBS pH 7.4, 1% Triton X-100 with protease inhibitor). The supernatant from this lysate was incubated with 2F2 anti-DEC-205 monoclonal antibodies for 16 hours at 4° C. while being stirred. Subsequently 30 μL of protein A-Sepharose (Pierce Rockford, Ill., USA) was used for immunoprecipitation, incubating for one hour at ambient temperature. The immune complexes that were formed were washed exhaustively with PBS-Tween 0.1%. The immunoprecipitates were eluted by boiling for five minutes in a sample buffer with SDS. The results are shown in FIG. 6, where the specific immunoisolation of the DEC-205 receptor (205 kDa) from cells present in the chicken spleen in a 10% SDS-PAGE gel under reduction conditions was observed, and the heavy chain (50 kDa) and the light chain (25 kDa) of the 2F2E8E3B6 antibody was observed with which immunoprecipitation was carried out. The molecular weights are indicated. This result indicates that the antibodies generated in this invention recognize the DEC-205 receptor that is present in the chicken (Gallus gallus) spleen cells based on the recognition of the CTLD-2 domain (SEQ ID NO:1).

Example 6 Internalization Test

The multi-lectin domains affect the efficiency of in vivo antigen processing and presentation; an indirect way of evaluating this process is to measure the internalization of anti-CTLD2 antibodies (SEQ ID NO:1) by the dendritic cells isolated from chicken spleens and by Jurkat cells. In general, 1×10E6 cells were stimulated with LPS for 24 hours and were then harvested, washed with PBS, and resuspended in 100 μL of 4% p-formaldehyde for 15 minutes at ambient temperature. After a second washing with PBS, resuspension was done in 100 μL of the permeabilization buffer 1× (Biolegend, CA, USA) for 20 minutes. The cells were blocked with species-specific serum (dilution 1:20) for 30 minutes at ambient temperature and were washed with PBS; they were then incubated for one hour with 26.7 μg/mL of the anti-CTLD2 antibody diluted in 1 mL of permeabilization buffer to ensure internalization thereof. The negative control used was the secondary antibody (anti-rat conjugated to phycoerythrin). The cells were washed and incubated with the secondary antibody (1:1000) for one hour. After the cells were washed with PBS, they were resuspended in 100 μL of 4% p-formaldehyde. A total of 10,000 cells for each condition, executed in triplicate, were analyzed on a FACSort (Becton-Dickinson, USA) using the FlowJo software. FIG. 7 shows the intracellular detection of the DEC-205 receptor in Jurkat cells that were permeabilized and stimulated with LPS using the murine monoclonal antibody 2F2E8E3B6 anti-CTLD-2 for detection thereof. The internalization of the DEC-205 receptor was done by stimulation with LPS up to 14% (FIG. 7B) compared to the control (3%) (FIG. 7A). This experiment was carried out in triplicate, where on average 13.5% of cells were observed to present internalization of the antibodies; this indicates that the phenomenon of internalization is indeed taking place.

Example 7 Cloning, Expression, and Purification of Hemagglutinin H5

RNA from the type H5N2 avian flu virus was obtained from a collection of RNAs donated by Dr. R. Webster (St. Jude Hospital, Tennessee, USA). H5 int R, H5 int F, HSR, and H5F oligonucleotides (SEQ ID NO: 9, 10, 11, and 12, respectively) were designed that flanked the hemagglutinin (H5) gene to amplify it by RT-PCR. The gene that codes for hemagglutinin H5 (SEQ ID NO: 8, reported in GenBank with access number gb|ABB88379.1) was cloned in the topo-TA amplification vector (Invitrogen), which was sequenced to confirm the viral origin of the hemagglutinin and to amplify it correctly. This gene was subcloned in the vector pFAST-BacHTb (Invitrogen), which adds six histodines that are contiguous to the amino-terminal region of hemagglutinin H5 (His₆-H5) and makes it possible to express it in insect cells. Once the pFAST Bac/H5 plasmid was obtained, it was transformed into DH10-bac cells in which, by double recombination, a recombinant bacmid was obtained that was capable of being transfected into insect cells of the Sf9 (Spodoptera frugiperda) and H5 (Trichopulsia ni) lines, to be subsequently expressed and purified. After infection for 24, 48, and 72 hours, the infected cells were washed with PBS and collected by centrifuging for 10 minutes at 10,000 RPM. The cells were treated with lysis buffer under native conditions (50 mM NaH₂PO₄, 300 mM NaCl, 10 mM imidazole, 1% Nonident P40 and protease inhibitor without EDTA) with incubation for 10 minutes at 4° C. After centrifuging was done, the clarified lysate was subjected to purification by means of Ni-NTA-Agarose affinity chromatography (Qiagen, USA), and the protein of interest was eluted by competency using a concentration gradient of up to 200 mM of imidazole. The His₆-H5 protein was monitored by 10% SDS-PAGE and Western-blot (FIG. 8); in the latter case anti-histidine antibodies were used (Pierce, Rockford, Ill., USA).

FIG. 8 shows a process of purification of hemagglutinin H5 (SEQ ID NO: 8) using a nickel-NTA-agarose column (Qiagen, USA) and carrying out dilution by competence with increasing concentrations of imidazole. This process was monitored by Western Blot, using anti-histidine antibodies united with peroxidase (Pierce, Rockford, Ill., USA) and revealed with an HRP Luminata Forte substrate (Millipore Corporation, Billerica). Trace 1) material not pegged to the nickel-agarose column; Trace 2) elution 1 with 50 mM of imidazole; Trace 3) elution 2 with 50 mM of imidazole; Trace 4) elution 1 with 100 mM of imidazole; Trace 5) elution 2 with 100 mM of imidazole; Trace 6) elution 1 with 150 mM of imidazole; Trace 7) elution 2 with 150 mM of imidazole; Trace 8) elution 1 with 200 mM of imidazole. Molecular weights of 70 and 130 kDa are noted. It is observed that the hemagglutinin H5 (SEQ ID NO: 8) with a molecular weight of 70 kDa is obtained at homogeneity with elution with 150 mM of imidazole, eliminating dimers and contaminants; this makes it possible to work with it for the subsequent conjugation processes.

Example 8 Chemical Conjugation of Hemagglutinin H5 (SEQ ID NO: 8) of the Avian Flu Virus with Anti-DEC205 Monoclonal Antibodies

The anti-CTLD-2 monoclonal antibodies, 2F2E8D3B6, at a concentration of 1 mg/mL, were activated with a 20× molar excess of the cross-linked agent SMCC (succinimidyl-4-(N-maleimidomethyl) cyclohexane-1-carboxylate (SMCC, Pierce, Rockford, Ill., USA) in PBS with 5 mM of EDTA for 2 hours at 4° C. This cross-linking agent contains an NHS ester group and a maleimide group that makes possible the covalent conjugation of the molecules that contain the amino groups and sulfhydryl groups, respectively. After activation, the samples were dialyzed against PBS in order to eliminate the reagent that had been released. On the other hand, the H5 recombinant protein that was obtained in the previous example was modified with 2-iminothiolane (Traut's Reagent, Pierce, Rockford, Ill., USA), which reacts with primary amines in order to add a sulfhydryl group to them. This modification was accomplished by incubating for 1 hour at ambient temperature the protein H5 at a concentration of 14.5 mg/mL in PBS, pH 8.0, with 5 mM of EDTA with a molar excess (10×) of Traut's Reagent, which was prepared at a concentration of 2 mg/mL. After the modification, the sample was dialyzed against PBS in order to eliminate the reagent that had been released. The activated antibodies and the modified protein were incubated for 12 hours at 4° C. in order to ensure covalent coupling thereof.

Example 9 Immunization of Hens with Antibody-Antigen (Anti-DEC-205-Hemagglutinin H5) Complexes

Two Rhode Island Red egg-laying hens, 25 weeks old, were immunized with the conjugate Ab 2F2E8D3B6-hemagglutinin H5 that was administered together with lipopolysaccharides (LPS) (SIGMA Aldrich, USA) at a ratio of 2:1. The immunization was given in a single dose of approximately 100 μg of conjugate for each hen, at a volume of 200 μL administered intradermally. The pre-immunization (prior to immunization) eggs and eggs laid during immunization were collected (for a period of 25 days), and they were kept at 4° C. until processed. Purification of the IgYs from the egg yolks was done to determine the titers of the anti-CTLD-2 chicken antibodies by the indirect ELISA method.

Example 10 Extraction, Purification of the IgY Antibodies, and Effect Determination as Modulators of the Immune Response in Chickens of the Antibody-Antigen (Anti-DEC-205 Antibodies-Hemagglutinin H5) Conjugates

The eggs of the immunized hens and those used as a control were subjected to manual extraction of the yolks, thus ensuring the release of the membranes that covered them. In general, 15 mL of yolk was obtained for each sample. Then the lipids present in the yolks were removed by separating the aqueous-organic phases using the PBS-chloroform suspension (one volume of chloroform to three volumes of PBS, pH 7.2). The aqueous phase was recovered so that it could be precipitated later with 50% saturated ammonium sulfate, while being stirred continuously and kept at 4° C. overnight. These samples were then centrifuged at 3000×g for 20 minutes at 4° C. in order to obtain the protein precipitate, which was reconstituted in 15 mL of PBS pH 7.2. This material was again precipitated with 30% saturation ammonium sulfate; after the processes of centrifuging and resuspension, all of the samples were subjected to dialysis against PBS pH 7.2, with various buffer changes being made over 24 hours. The concentrations of the proteins extracted from the egg yolks were determined by absorbency at 280 nm. Titration of the anti-hemagglutinin H5 chicken antibodies was done by the indirect ELISA method using 0.3 μg/well of antigen H5 (SEQ ID NO: 8) and a secondary anti-chicken antibody united with peroxidase (dilution 1:2500, Pierce, Rockford, Ill.). The results are presented in FIG. 9, which indicates the IgY titers that recognize hemagglutinin H5 (SEQ ID NO: 8) of the avian flu virus in the two immunized hens on days 15, 18, and 21 post immunization. The hens successfully generated antibodies that were capable of recognizing the viral protein with larger titers than with the control starting on day 15 (titers above 2500) with a single immunization, confirming that the anti-CTLD-2-hemagglutinin H5 conjugates of this invention have the potential to be used as regulators of the immune response in chickens (Gallus gallus) to prevent possible viral infections. These results were compared with normal immunization schemes in chickens where in general titers greater than 2000 begin to be obtained as of the fifth week of immunization and after various reinforcement measures (Wen et al., 2012).

Example 11 Recognition of the CTLD2 Domain of DEC 205 in Other Species

In order to analyze whether the antibodies produced recognize the DEC-205 receptor in other species, immunoprecipitation tests were run on species other than chickens (Gallus gallus). For this purpose Jurkat cells (the cell line of human T lymphocytes) as well as white cells obtained from the spleens of different animals (pigs and dogs) were lysed in an immunoprecipitation buffer (PBS pH 7.4, 1% Triton X-100 with protease inhibitor). The supernatants of these lysates were incubated with the anti-DEC-205 monoclonal antibodies for 16 hours at 4° C. while being stirred. Then, 50 μL of A-Sepharose protein (Pierce, Rockford, Ill., USA) was used for immunoprecipitation, with incubation being done for one hour at ambient temperature. The immune complexes that were formed were washed extensively. The immunoprecipitates were eluted by boiling for five minutes in a sample buffer with SDS. These precipitates were analyzed on a 10% SDS-PAGE gel under reducing conditions using molecular weight markers. The results are shown in FIG. 10A, where the specific immunoisolation is observed of the DEC-205 receptor (205 kDa) present in Jurkat cells (immortalized line of T lymphocytes) of Homo sapiens and white cells of pigs spleens (Sus scrofa) in a 10% SDS-PAGE gel under reducing conditions (this was not observed when dog spleen cells were used). The heavy chain (50 kDa) and light chain (25 kDa) of the 2F2E8E3B6 antibody were observed with which the immunoprecipitation was done. The molecular weights are indicated. FIG. 10B shows the alignment of sequences of the CTLD-2 segment of the lymphocytic antigen 75 (DEC-205) of Gallus gallus (NP_001032925.1) compared to the sequences of Homo sapiens (NP_002340.2) and pig (Sus scrofa) (NP_001171875.1), as well as the percentage of identity thereof. It is observed that the two domains exhibit 65% identity compared to the chicken (Gallus gallus) domain; this percentage is sufficient to establish the molecular recognition observed in the immunoprecipitation processes.

Example 12 Sequencing of the Variable Regions of the Anti-DEC205 Antibodies

As described in Example 3, the murine antibodies that specifically recognize the CTLD-2 domain of the DEC-205 receptor were purified by means of affinity chromatography with Protein A. The purified antibodies were transferred to nitrocellulose membranes to determine the amino-terminal sequences of the variable regions of the heavy and light chains by means of Edman degradation in a PPSQ-31A sequencer (Shimadzu, Kyoto, Japan). Once this sequence was obtained, the oligos of the amino-terminal regions (SEQ ID NO. 17, 19, 21, and 22) were designed. The oligo is that were used to amplify the carboxyl-terminal regions of the heavy and light chains were taken from specific sites where the constant chains of the two chains began in accordance with the previously obtained isotype; for the case of the light kappa chain, the oligo (SEQ ID NO. 20) reported in Yuan et al., 2004, was used; for the case of the light lambda chain, the oligo (SEQ ID NO. 18) reported in Miller and Glasel, 1989 was used. The oligo for the hinge regions (SEQ ID NO. 23) of the heavy chains was produced in accordance with the consensus sequence of the hinge regions.

The sequences of the regions of the heavy and light chains (VH and VL) of the antibodies originating from the 2F2 and 4D12R hybridomas were identified using the RNA of these hybridomas, which was purified using the “SV Total RNA Isolation” kit (Promega, Madison, USA). The cDNA was obtained by reverse transcription from the RNA using the reverse transcriptase enzyme Expand (Roche Applied Science, Germany). The variable regions were amplified by PCR, where the products were separated on a 1% agarose gel and were purified with the QIAQuick gel extraction kit (Qiagen, USA). These products were ligated using the T4 DNA ligase enzyme (Fermentas, Canada) and were cloned in the cloning vector pBlueScriptks (−) (previously directed with the EcoRV enzyme, Stratagene, USA). The ligation product was transformed into DH5α chemical-competent cells. The transformed cells were plated in petri dishes with YT2X medium fortified with 50 μg/mL of ampicillin, IPTG/XGal for the selection of positive (white) colonies. The cloning of the heavy and light chains was verified by means of colony PCR using the oligos of the vector, T7-like (SEQ ID NO. 24) and T3-like (SEQ ID NO. 25). The colonies having the inserts of the desired sizes (for VH's 750 pb and for VL's 600 pb) were amplified, and the plasmid DNA was purified with the “High Pure Plasmid Isolation” kit (Roche Applied Science, Germany). Then the sequencing of the DNA of the plasmids was done on an Applied Biosystems 3100 gene analyzer (Foster City, Calif., USA). The sequences of the variable regions of the light and heavy chains of the antibody 2F2E8E3B6 (SEQ ID NO. 13 and 15) and of the 4D12R antibody (SEQ ID NO. 14 and 16) were obtained, as was the definition of the complementarity-determining regions (CDRs) of each chain in accordance with the Kabat nomenclature (http://www.bioinf.org.uk/abs/); these are the ones that specifically recognize the CTLD-2 region of the DEC-205 receptor. The heavy (V_(H)) chains present at the CDR1_(H) of amino acids 26-35,at the CDR2_(H) of amino acids 50-65, and at the CDR3_(H) of amino acids 99-103; the light chains present at CDR1_(L) of amino acids 24-40, at CDR2_(L) of amino acids 56-62, and at CDR3_(L) of amino acids 95-102. 

1. An antibody that recognizes the CTLD-2 domain of the DEC-205 receptor of Gallus gallus (SEQ ID NO. 1), characterized by the fact that it comprises a fragment V_(H) with an amino acid sequence selected from the group that consists of SEQ ID NO. 15, SEQ ID NO. 16, and functionally equivalent variants in positions 26-35, 50-65, and 99-103 of said SEQ ID NO. 15 or SEQ ID NO. 16 and a fragment V_(L) with a sequence selected from the group consisting of SEQ ID NO. 13 and SEQ ID NO. 14, and functionally equivalent variants in positions 24-40, 56-62, or 95-102 of said SEQ ID NO. 13 or SEQ ID NO.
 14. 2. An antibody in accordance with claim 1, characterized by the fact that it comprises a fragment V_(H) with an amino acid sequence SEQ ID NO. 15 and a fragment V_(L) with an amino acid sequence SEQ ID NO.
 13. 3. An antibody in accordance with claim 1, characterized by the fact that it comprises a fragment V_(H) with an amino acid sequence SEQ ID NO. 16 and a fragment V_(L) with an amino acid sequence SEQ ID NO.
 14. 4. A molecular conjugate of the antibody of claim 1 that recognizes the CTLD-2 domain of the DEC-205 receptor of Gallus gallus, characterized by the fact that the antibody is covalently united to an antigen.
 5. The molecular conjugate of claim 4, characterized by the fact that the antigen is a protein that is selected from the group that consists of proteins selected from the bacteria Pastuerella multocida of avian cholera, Avibacterium paragallinarum of infectious avian coryza, the avian viral leukosis virus, and the avian flu virus.
 6. The molecular conjugate of claim 5, characterized by the fact that the protein used as an antigen is selected from the group that consists of the Cp39 protein of Pastuerella multocida, the protein of the HMTp210 external membrane of Avibacterium paragallinarum, the gp85 protein of avian leukosis subgroup J, and the H5 protein of the avian flu virus.
 7. The molecular conjugate of claim 6, characterized by the fact that the conjugate antigen is the H5 protein of the avian flu virus of amino-acid sequence SEQ ID NO:
 8. 8. The molecular conjugate of claim 4, characterized by the fact that the antibody comprises a fragment V_(H) with an amino-acid sequence SEQ ID NO: 15 and a fragment V_(L) with an amino-acid sequence SEQ ID NO:
 13. 9. The molecular conjugate of claim 4, characterized by the fact that the antibody comprises a fragment V_(H) with an amino-acid sequence SEQ ID NO: 16 and a fragment V_(L) with an amino-acid sequence SEQ ID NO:
 14. 10. The use of a molecular conjugate in accordance with claim 4 to fabricate a veterinary vaccine against avian cholera, avian infectious coryza, avian leukosis subgroup J, and avian influenza.
 11. The use of a molecular conjugate in accordance with claim 7 to fabricate a veterinary vaccine against avian influenza.
 12. A veterinary compound for preventing avian illnesses, characterized by the fact that it comprises a molecular conjugate in accordance with claim 5, or a salt of said pharmaceutically acceptable compound, and a pharmaceutically acceptable vehicle.
 13. The composition of claim 12, characterized by the fact that the avian illness is influenza and the molecular conjugate that it comprises is in accordance with claim
 7. 14. The use of a molecular conjugate in accordance with claim 5 to fabricate a veterinary vaccine against avian cholera, avian infectious coryza, avian leukosis subgroup J, and avian influenza.
 15. The use of a molecular conjugate in accordance with claim 6 to fabricate a veterinary vaccine against avian cholera, avian infectious coryza, avian leukosis subgroup J, and avian influenza.
 16. The use of a molecular conjugate in accordance with claim 8 to fabricate a veterinary vaccine against avian influenza.
 17. The use of a molecular conjugate in accordance with claim 9 to fabricate a veterinary vaccine against avian influenza.
 18. A veterinary compound for preventing avian illnesses, characterized by the fact that it comprises a molecular conjugate in accordance with claim 6, or a salt of said pharmaceutically acceptable compound, and a pharmaceutically acceptable vehicle.
 19. A veterinary compound for preventing avian illnesses, characterized by the fact that it comprises a molecular conjugate in accordance with claim 7, or a salt of said pharmaceutically acceptable compound, and a pharmaceutically acceptable vehicle. 